Senior QA Auditor - GCP Audits

IQVIA; Glendale (AZ); On-site; USD 75,000 - 189,000; Full time

Job summary

IQVIA is hiring for a Quality Assurance Auditor to independently lead audit activities across diverse clinical research programs. You will collaborate with global teams to ensure compliance with GCP, guidelines, and SOPs while promoting continuous improvement.

The role requires extensive QA auditing experience, strong communication, and the ability to work across regions with minimal supervision. Travel is expected 30-50% to sites worldwide.

Qualifications

• Experience in the conduct of clinical trial Investigator Site Audits.
• Travel 30-50%.
• 5 years experience in pharmaceutical, technical, or related area, with 3 years in QA Audits.
• GCP experience.
• Knowledge of pharmaceutical R&D processes, regulatory environments, and QA processes.

Responsibilities

• Plan, schedule, conduct, report and close audit activities across IQVIA contracts.
• Evaluate audit findings and prepare reports for stakeholders.
• Provide interpretation of regulations and guidance to project teams.
• Develop CAPA plans and track their closure.
• Review investigations, RCA, CAPA and EC plans and ensure effectiveness.

Skills

Travel flexibility

GCP experience

Quality Assurance Audits

Interpersonal skills

Problem solving

Risk analysis

Project management

Communication

Education

Bachelor's Degree

Tools

Word processing

Spreadsheet

Database applications

Job description

Durham, North Carolina, United States of America

Indianapolis, IN, United States of America

Parsippany, New Jersey, United States of America

Wayne, PA, United States of America

Glendale, AZ, United States of America

Full time

R1527130

Overview

Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines, policies, and procedures. Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies.

This role offers the opportunity to independently lead audit activities across a diverse portfolio of clinical research programs and collaborate with global teams to support quality, compliance, and continuous improvement initiatives.

Core Responsibilities

• Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions.

• Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers.

• Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures.

• Provide consultation to customers and monitors in interpretation of audit observations and formulation of Corrective and Preventive Action (CAPA) plans.

• Review, approve investigations, Root Cause Analysis (RCA), CAPA and Effectiveness Check (EC) plans and track till closure for quality events arising from Audits; and from Quality Issues, Inspections or during similar QA activities as assigned.

• Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements.

• Perform pre-inspection visits at sites.

• Maintain the electronic quality management system (eQMS) and provide support in relation to the audit lifecycle.

• Lead, collaborate in, or support QA initiatives and process improvement projects.

Additional Responsibilities

Depending on business needs, the role may also include:

• Assist in training of new Quality Assurance staff.

• Manage Quality Issues.

• Present educational programs and provide guidance to operational staff on compliance procedures.

• As assigned, host audits/inspections, ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections.

Required Qualifications

Experience in the conduct of clinical trial Investigator Site Audits.

• Travel 30-50%.

• 5 years experience in pharmaceutical, technical, or related area, of which 3 years in Quality Assurance Audits.

• GCP experience.

• Extensive knowledge of pharmaceutical research and development processes, regulatory environments, and quality assurance processes and procedures.

• Strong interpersonal skills and excellent problem solving, risk analysis and negotiation skills.

• Strong training capabilities and ability to initiate assigned tasks and work independently.

• Effective organization, communication and team orientation skills, with ability to manage multiple projects and establish and maintain effective working relationships with coworkers, managers and clients.

• Knowledge of word-processing, spreadsheet, and database applications.

Preferred Qualifications (Beneficial but Not Essential)

• Experience in the conduct of clinical study report / data management clinical trial audits.

• Bachelor's Degree.

Why Join IQVIA Quality Assurance?

• Independently lead the full audit lifecycle across a diverse portfolio of clinical research programs.

• Work within a global quality organization supporting international clinical research activities.

• Collaborate with experienced QA professionals and cross-functional teams across regions.

• Contribute to quality and compliance initiatives that support continuous improvement and operational excellence.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $75,400.00 - $188,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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